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首页> 外文期刊>Journal of the Chemical Society of Pakistan >Synthesis and Biological Significances of New Heterocyclic Compounds Containing 5-(4-Chlorobenzyl)-3-(4-Chlorophenyl)-1H-1,2,4-triazol Ring
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Synthesis and Biological Significances of New Heterocyclic Compounds Containing 5-(4-Chlorobenzyl)-3-(4-Chlorophenyl)-1H-1,2,4-triazol Ring

机译:含有5-(4-氯苄基)-3-(4-氯苯基)-1H-1,2,4-三唑环的新型杂环化合物的合成及生物学意义

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摘要

In this study, some novel 5-(4-chlorobenzyl)-3-(4-chlorophenyl)-1H-1,2,4-triazol derivatives were synthesized starting from 4-amino-3-(4-chlorobenzyl)-5-(4- chlorophenyl)-4H-1,2,4- triazole (1). The structures of the synthesized compounds were clarified using IR, H-1 NMR, C-13 NMR, elemental analyses and mass spectral techniques. The synthesized compounds were tested for antimicrobial and anti-lipase inhibitory activities. Among the tested substances, compounds 3, 8c, 8d, 8e and 9d exhibited good activity against Gram-positive bacteria. Furthermore, all the synthesized compounds were investigated with regard to pancreatic lipase inhibition activity, and compounds 5e, 8b, and 9b showed a considerable anti-lipase activity at various concentrations.
机译:在该研究中,从4-氨基-3-(4-氯苄基)-5-开始,合成了一些新的5-(4-氯苄基)-3-(4-氯苯基)-1H-1,2,4-三唑衍生物。 (4-氯苯基)-4H-1,2,4-三唑(1)。 使用IR,H-1 NMR,C-13 NMR,元素分析和质谱技术澄清合成化合物的结构。 测试合成化合物以进行抗微生物和抗脂肪酶抑制活性。 在测试的物质中,化合物3,8C,8D,8E和9D对革兰氏阳性细菌表现出良好的活性。 此外,关于胰脂肪酶抑制活性研究所有合成的化合物,化合物5e,8b和9b在各种浓度下显示出相当大的抗脂肪酶活性。

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